HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58343Generated: October 25, 2026
1,1'-Carbonyldiimidazole → 8,8,11,14,14-Pentamethyl-7,12-dioxo-1,1,1-triphenyl-13-oxa-6,11-diaza-1-phosphoniapentadecane bromide
https://huagongshe.com/reaction/58343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | (4-Aminobutyl)(triphenyl)phosphonium bromide | HCID 10201848 | — |
| Reactant | 4-[(Tert-butoxycarbonyl)(methyl)amino]-2,2-dimethylbutanoic acid | HCID 54754482 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8,8,11,14,14-Pentamethyl-7,12-dioxo-1,1,1-triphenyl-13-oxa-6,11-diaza-1-phosphoniapentadecane bromide | HCID 89463368 | 69% |
Reaction Steps
4-[(tert-butoxycarbonyl)(methyl)amino]-2,2-dimethylbutanoic acid (Organic and Molecular Chemistry, 2011, 9, 1846-1854, 117 mg, 0.48 mmol) was dissolved in N,N-dimethylformamide (1.2 mL) and treated with N,N-carbonyldiimidazole (104 mg, 0.64 mmol). The mixture was stirred at room temperature for 30 minutes. (4-Aminobutyl)(triphenyl)phosphonium bromide (277 mg, 0.67 mmol) was added, and the reaction was stirred overnight at room temperature. The reaction mixture was then diluted with methylene chloride and washed with 5% aqueous lithium chloride (3 times), 1N aqueous hydrogen chloride, and saturated sodium bicarbonate. The organic solution was dried over anhydrous sodium sulfate, filtered, and concentrated to give the title compound (210 mg, 69%) as a white foam. Sample was used crude in next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434753B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-b462afc41980416ea4c8e455f09a0e8c |
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| Source note | uspto-grants-2016_09 |
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